Rare lichen planus
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Rare LP |
| Number of Symptoms | 3 |
| OrphanetNr: | 254367 |
| OMIM Id: |
151620
|
| ICD-10: |
L43 L66.1 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant inheritance [Omim] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Epidermal disease
-Rare skin disease |
Symptom Information:
|
|
(HPO:0000951) | Abnormality of the skin | 147 / 7739 | ||||
|
|
(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
|
|
(MedDRA:10024429) | Lichen planus | 1 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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